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Hypenia salzmannii

Hypenia salzmannii - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643fdf5b9de68186830741
Scientific name Hypenia salzmannii
Authority (Benth.) Harley
First published in Bot. J. Linn. Soc. 98(2): 91 (1988):.

Description Top

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Synonyms Top

Scientific name Authority First published in
Hyptis salzmannii Benth. Labiat. Gen. Spec. : 138 (1833)
Hyptis salzmannii var. filipes Benth. Prodr. 12: 137 (1848)
Hyptis salzmannii var. tomentosa Benth. Labiat. Gen. Spec. : 138 (1833)
Mesosphaerum salzmannii Kuntze Revis. Gen. Pl. 2: 527 (1891)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000216208
Tropicos 50168400
KEW urn:lsid:ipni.org:names:278563-2
The Plant List kew-101342
Open Tree Of Life 642520
NCBI Taxonomy 986192
IPNI 945655-1
iNaturalist 867678
GBIF 3883818
EOL 5370865

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Application of Rosmarinic Acid with Its Derivatives in the Treatment of Microbial Pathogens Kernou ON, Azzouz Z, Madani K, Rijo P Molecules 22-May-2023
PMCID:PMC10220798
doi:10.3390/molecules28104243
PMID:37241981
A Comprehensive Review of Rosmarinic Acid: From Phytochemistry to Pharmacology and Its New Insight Guan H, Luo W, Bao B, Cao Y, Cheng F, Yu S, Fan Q, Zhang L, Wu Q, Shan M Molecules 20-May-2022
PMCID:PMC9143754
doi:10.3390/molecules27103292
PMID:35630768
Machine Learning Analysis of Essential Oils from Cuban Plants: Potential Activity against Protozoa Parasites Barros de Menezes RP, Scotti L, Scotti MT, García J, González R, Monzote L, Setzer WN Molecules 17-Feb-2022
PMCID:PMC8878085
doi:10.3390/molecules27041366
PMID:35209156
Trypanocidal Essential Oils: A Review de Morais MC, de Souza JV, da Silva Maia Bezerra Filho C, Dolabella SS, de Sousa DP Molecules 06-Oct-2020
PMCID:PMC7583723
doi:10.3390/molecules25194568
PMID:33036315
Subtribe Hyptidinae (Lamiaceae): A promising source of bioactive metabolites Bridi H, de Carvalho Meirelles G, Lino von Poser G J Ethnopharmacol 05-Aug-2020
PMCID:PMC7403033
doi:10.1016/j.jep.2020.113225
PMID:32763419
Active Essential Oils and Their Components in Use against Neglected Diseases and Arboviruses Luna EC, Luna IS, Scotti L, Monteiro AF, Scotti MT, de Moura RO, de Araújo RS, Monteiro KL, de Aquino TM, Ribeiro FF, Mendonça FJ Junior Oxid Med Cell Longev 07-Feb-2019
PMCID:PMC6387720
doi:10.1155/2019/6587150
PMID:30881596
The “Hidden Diversity” of Medicinal Plants in Northeastern Brazil: Diagnosis and Prospects for Conservation and Biological Prospecting Cavalcanti DR, Albuquerque UP Evid Based Complement Alternat Med 20-Oct-2013
PMCID:PMC3817947
doi:10.1155/2013/102714
PMID:24228056
Which Approach Is More Effective in the Selection of Plants with Antimicrobial Activity? Silva AC, Santana EF, Saraiva AM, Coutinho FN, Castro RH, Pisciottano MN, Amorim EL, Albuquerque UP Evid Based Complement Alternat Med 26-Jun-2013
PMCID:PMC3710641
doi:10.1155/2013/308980
PMID:23878595
(−)-Salzol, an isopimarane diterpene, and a chalcone from Hyptis salzmanii Irene Messana, Franco Ferrari, Maria Alves de Moraes e Souza, Eszter Gács-Baitz Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)89065-H

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Lignans, neolignans and related compounds / Furanoid lignans
Sesamin 72307 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1016/0031-9422(90)89065-H
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactols
Cubebin 117443 Click to see C1C(C(C(O1)O)CC2=CC3=C(C=C2)OCO3)CC4=CC5=C(C=C4)OCO5 356.40 unknown https://doi.org/10.1016/0031-9422(90)89065-H
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
Hinokinin 442879 Click to see C1C(C(C(=O)O1)CC2=CC3=C(C=C2)OCO3)CC4=CC5=C(C=C4)OCO5 354.40 unknown https://doi.org/10.1016/0031-9422(90)89065-H
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
4-Methoxycinnamic acid 13245 Click to see COC1=CC=C(C=C1)C=CC(=O)O 178.18 unknown https://doi.org/10.1016/0031-9422(90)89065-H
trans-4-Methoxycinnamic acid 699414 Click to see COC1=CC=C(C=C1)C=CC(=O)O 178.18 unknown https://doi.org/10.1016/0031-9422(90)89065-H
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Isosakuranetin 160481 Click to see COC1=CC=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O 286.28 unknown https://doi.org/10.1016/0031-9422(90)89065-H

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